A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275428



Internal ID20842468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5927155..6797765hg38UCSC Ensembl
chr7:5966786..6837396hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38870611
hg19870611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570632
Supporting Variants
Samples
Known GenesAIMP2, ANKRD61, C7orf26, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, PMS2, PMS2CL, RAC1, RSPH10B, RSPH10B2, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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